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BioWorld - Wednesday, December 24, 2025
Home » Topics » Infection » Coronavirus

Coronavirus
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Remdesivir vial and syringe

With limited options, US FDA aims at omicron by expanding Veklury use

Jan. 24, 2022
By Mari Serebrov
Once again, the U.S. FDA giveth and it taketh away. Just a few days after expanding its approval for Gilead Sciences Inc.’s Veklury (remdesivir) to provide access to more people infected with COVID-19, the FDA essentially shut down the use of two monoclonal antibody (mAb) treatments Jan. 24 that had been authorized to treat mild-to-moderate COVID-19 infections – Regeneron Inc.’s Regen-Cov (Ronapreve in Europe), an antibody cocktail of casirivimab and imdevimab, and Eli Lilly and Co.’s bamlanivimab and etesevimab that are administered together.
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Sanofi-backed Protas plans new tack on costly trials enterprise

Jan. 24, 2022
By Nuala Moran
LONDON – A pledge to “bottle” improvements made in setting up and running clinical trials during the pandemic has materialized in the formation of Protas Ltd., a nonprofit promising to stage large-scale phase III clinical trials in common diseases for less than one tenth the current cost. Protas will design and run randomized phase III studies of new and repurposed drugs in conditions including depression, dementia, heart, lung and respiratory conditions, arthritis and cancer.
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Other news to note for Jan. 24, 2022

Jan. 24, 2022
Biopharma happenings, including deals and partnerships, grants, preclinical data and other news in brief: Anixa, Arrowhead, Dnovo, GSK, Molgenie, Neoimmunetech, Opthea, Respirerx.
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In the clinic for Jan. 24, 2022

Jan. 24, 2022
Clinical updates, including trial initiations, enrollment status and data readouts and publications: Aslan, Clover, Opiant, Provention, UCB.
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Regulatory actions for Jan. 21, 2022

Jan. 21, 2022
Regulatory snapshots, including global submissions and approvals, clinical trial approvals and other regulatory decisions and designations: Seegene.
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Regulators call for multivalent COVID-19 shots, not endless boosters

Jan. 21, 2022
By Richard Staines
Administering multiple booster doses against COVID-19 is not sustainable in the longer term, international drug regulators said during a meeting of the International Coalition of Medicines Regulatory Authorities, held Jan. 12. Regulators argued that a long-term strategy should involve vaccines capable of tackling several variants at once, not just omicron, and that tweaking existing vaccines and comparing them with first-generation vaccines using clinical studies is the way forward, according to a report from the meeting.
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Regulatory actions for Jan. 21, 2022

Jan. 21, 2022
Regulatory snapshots, including global drug submissions and approvals, clinical trial approvals and other regulatory decisions and designations: AB Science, Amgen, AN2, Aptorum, Argenx, Beigene, Betterlife, Clairvoyant, Compass, Idorsia, Jeil, Marker, Novavax, Nuvation, Omeros, Opko, Palleon, Pfizer, Rockwell, Senhwa, Turning Point.
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Other news to note for Jan. 21, 2022

Jan. 21, 2022
Biopharma happenings, including deals and partnerships, grants, preclinical data and other news in brief: Alzinova, MD Anderson, Orchard, Revivicor, Sorrento, Tevogen, Trisalus, United Therapeutics, Yingli.
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In the clinic for Jan. 21, 2022

Jan. 21, 2022
Clinical updates, including trial initiations, enrollment status and data readouts and publications: Arecor, Biovie, Calcimedica, Elpiscience, Hinova, Hutchmed, Idorsia, Infant Bacterial, Intelgenx, Merck, Oncolytic, Revelation, Seres, Sorrento, Vigeo, Xilio, Zealand.
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Earth infected with pandemic

Targetingone digital PCR testing kit wins first-of-kind class III Chinese approval

Jan. 20, 2022
By Zhang Mengying
Targetingone Corp. Ltd.’s new testing kit based on digital polymerase chain reaction (dPCR) techniques has received approval from China’s NMPA. It is the first dCPR-based testing kit to receive the country’s class III medical device registration certificate. The Beijing-based company collaborated with Tsinghua University, several hospitals and the Chinese Center for Disease Control and Prevention (CDC) participated to research and develop the testing kit.
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